"Hyperoxaluria, Primary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
| Descriptor ID |
D006960
|
| MeSH Number(s) |
C12.777.419.313.500 C13.351.968.419.313.500 C16.320.565.202.460 C18.452.648.202.460
|
| Concept/Terms |
Hyperoxaluria, Primary- Hyperoxaluria, Primary
- Hyperoxalurias, Primary
- Primary Hyperoxalurias
- Primary Hyperoxaluria
- Primary Oxaluria
- Oxaluria, Primary
- Oxalurias, Primary
- Primary Oxalurias
Primary Oxalosis- Primary Oxalosis
- Oxaloses, Primary
- Oxalosis, Primary
- Primary Oxaloses
|
Below are MeSH descriptors whose meaning is more general than "Hyperoxaluria, Primary".
- Diseases [C]
- Male Urogenital Diseases [C12]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Hyperoxaluria [C12.777.419.313]
- Hyperoxaluria, Primary [C12.777.419.313.500]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Hyperoxaluria [C13.351.968.419.313]
- Hyperoxaluria, Primary [C13.351.968.419.313.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
- Hyperoxaluria, Primary [C16.320.565.202.460]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
- Hyperoxaluria, Primary [C18.452.648.202.460]
Below are MeSH descriptors whose meaning is more specific than "Hyperoxaluria, Primary".
This graph shows the total number of publications written about "Hyperoxaluria, Primary" by people in this website by year, and whether "Hyperoxaluria, Primary" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2020 | 1 | 0 | 1 |
| 2021 | 2 | 0 | 2 |
| 2022 | 2 | 0 | 2 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperoxaluria, Primary" by people in Profiles.
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Diagnosis and management of primary hyperoxalurias: best practices. Pediatr Nephrol. 2024 Nov; 39(11):3143-3155.
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Efficacy and safety of lumasiran for infants and young children with primary hyperoxaluria type 1: 12-month analysis of the phase 3 ILLUMINATE-B trial. Pediatr Nephrol. 2023 04; 38(4):1075-1086.
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Lumasiran for Advanced Primary Hyperoxaluria Type 1: Phase 3 ILLUMINATE-C Trial. Am J Kidney Dis. 2023 Feb; 81(2):145-155.e1.
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Phase 3 trial of lumasiran for primary hyperoxaluria type 1: A new RNAi therapeutic in infants and young children. Genet Med. 2022 03; 24(3):654-662.
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Posttransplant recurrence of calcium oxalate crystals in patients with primary hyperoxaluria: Incidence, risk factors, and effect on renal allograft function. Am J Transplant. 2022 01; 22(1):85-95.
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Recovery From Dialysis in Patients With Primary Hyperoxaluria Type 1 Treated With Pyridoxine: A Report of 3 Cases. Am J Kidney Dis. 2021 05; 77(5):816-819.
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Invited response to recurrence of oxalate nephropathy after isolated kidney transplantation for primary hyperoxaluria type 2. Am J Transplant. 2018 02; 18(2):527.
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Combined Liver-Kidney Transplantation for Primary Hyperoxaluria Type 2: A Case Report. Am J Transplant. 2018 01; 18(1):253-257.
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Progressive polyradiculoneuropathy due to intraneural oxalate deposition in type 1 primary hyperoxaluria. Muscle Nerve. 2015 Mar; 51(3):449-54.
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Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplant. Am J Transplant. 2014 Jun; 14(6):1433-8.